Canonical Allele Identifier: CA2466807539

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154837960_154837962delinsTAC , CM000685.2:g.154837960_154837962delinsTAC	GRCh38
NC_000023.10:g.154066235_154066237delinsTAC , CM000685.1:g.154066235_154066237delinsTAC	GRCh37
NC_000023.9:g.153719429_153719431delinsTAC	NCBI36
NG_011403.1:g.189762_189764delinsGTA
NG_033065.1:g.1701_1703delinsGTA
NG_011403.2:g.189762_189764delinsGTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.6901-210_6901-208delinsGTA MANE Select	ENSP00000353393.4:n.6901-210_6901-208delinsGTA
ENST00000644698.1:c.634-210_634-208delinsGTA	ENSP00000495706.1:n.634-210_634-208delinsGTA
ENST00000330287.10:c.496-210_496-208delinsGTA	ENSP00000327895.6:n.496-210_496-208delinsGTA
ENST00000360256.8:c.6901-210_6901-208delinsGTA	ENSP00000353393.4:n.6901-210_6901-208delinsGTA
NM_000132.3:c.6901-210_6901-208delinsGTA	NP_000123.1:n.6901-210_6901-208delinsGTA
NM_019863.2:c.496-210_496-208delinsGTA	NP_063916.1:n.496-210_496-208delinsGTA
XM_011531126.1:c.6796-210_6796-208delinsGTA	XP_011529428.1:n.6796-210_6796-208delinsGTA
NM_000132.4:c.6901-210_6901-208delinsGTA MANE Select	NP_000123.1:n.6901-210_6901-208delinsGTA
NM_019863.3:c.496-210_496-208delinsGTA	NP_063916.1:n.496-210_496-208delinsGTA